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Subset- and tissue-defined STAT5 thresholds control homeostasis and function of innate lymphoid cells

Innate lymphoid cells (ILCs) patrol environmental interfaces to defend against infection and protect barrier integrity. Using a genetic tuning model, we demonstrate that the signal-dependent transcription factor (TF) STAT5 is critical for accumulation of all known ILC subsets in mice and reveal a hi...

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Autores principales: Villarino, Alejandro V., Sciumè, Giuseppe, Davis, Fred P., Iwata, Shigeru, Zitti, Beatrice, Robinson, Gertraud W., Hennighausen, Lothar, Kanno, Yuka, O’Shea, John J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626390/
https://www.ncbi.nlm.nih.gov/pubmed/28916644
http://dx.doi.org/10.1084/jem.20150907
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author Villarino, Alejandro V.
Sciumè, Giuseppe
Davis, Fred P.
Iwata, Shigeru
Zitti, Beatrice
Robinson, Gertraud W.
Hennighausen, Lothar
Kanno, Yuka
O’Shea, John J.
author_facet Villarino, Alejandro V.
Sciumè, Giuseppe
Davis, Fred P.
Iwata, Shigeru
Zitti, Beatrice
Robinson, Gertraud W.
Hennighausen, Lothar
Kanno, Yuka
O’Shea, John J.
author_sort Villarino, Alejandro V.
collection PubMed
description Innate lymphoid cells (ILCs) patrol environmental interfaces to defend against infection and protect barrier integrity. Using a genetic tuning model, we demonstrate that the signal-dependent transcription factor (TF) STAT5 is critical for accumulation of all known ILC subsets in mice and reveal a hierarchy of STAT5 dependency for populating lymphoid and nonlymphoid tissues. We apply transcriptome and genomic distribution analyses to define a STAT5 gene signature in natural killer (NK) cells, the prototypical ILC subset, and provide a systems-based molecular rationale for its key functions downstream of IL-15. We also uncover surprising features of STAT5 behavior, most notably the wholesale redistribution that occurs when NK cells shift from tonic signaling to acute cytokine-driven signaling, and genome-wide coordination with T-bet, another key TF in ILC biology. Collectively, our data position STAT5 as a central node in the TF network that instructs ILC development, homeostasis, and function and provide mechanistic insights on how it works at cellular and molecular levels.
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spelling pubmed-56263902017-10-05 Subset- and tissue-defined STAT5 thresholds control homeostasis and function of innate lymphoid cells Villarino, Alejandro V. Sciumè, Giuseppe Davis, Fred P. Iwata, Shigeru Zitti, Beatrice Robinson, Gertraud W. Hennighausen, Lothar Kanno, Yuka O’Shea, John J. J Exp Med Research Articles Innate lymphoid cells (ILCs) patrol environmental interfaces to defend against infection and protect barrier integrity. Using a genetic tuning model, we demonstrate that the signal-dependent transcription factor (TF) STAT5 is critical for accumulation of all known ILC subsets in mice and reveal a hierarchy of STAT5 dependency for populating lymphoid and nonlymphoid tissues. We apply transcriptome and genomic distribution analyses to define a STAT5 gene signature in natural killer (NK) cells, the prototypical ILC subset, and provide a systems-based molecular rationale for its key functions downstream of IL-15. We also uncover surprising features of STAT5 behavior, most notably the wholesale redistribution that occurs when NK cells shift from tonic signaling to acute cytokine-driven signaling, and genome-wide coordination with T-bet, another key TF in ILC biology. Collectively, our data position STAT5 as a central node in the TF network that instructs ILC development, homeostasis, and function and provide mechanistic insights on how it works at cellular and molecular levels. The Rockefeller University Press 2017-10-02 /pmc/articles/PMC5626390/ /pubmed/28916644 http://dx.doi.org/10.1084/jem.20150907 Text en This is a work of the U.S. Government and is not subject to copyright protection in the United States. Foreign copyrights may apply. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Articles
Villarino, Alejandro V.
Sciumè, Giuseppe
Davis, Fred P.
Iwata, Shigeru
Zitti, Beatrice
Robinson, Gertraud W.
Hennighausen, Lothar
Kanno, Yuka
O’Shea, John J.
Subset- and tissue-defined STAT5 thresholds control homeostasis and function of innate lymphoid cells
title Subset- and tissue-defined STAT5 thresholds control homeostasis and function of innate lymphoid cells
title_full Subset- and tissue-defined STAT5 thresholds control homeostasis and function of innate lymphoid cells
title_fullStr Subset- and tissue-defined STAT5 thresholds control homeostasis and function of innate lymphoid cells
title_full_unstemmed Subset- and tissue-defined STAT5 thresholds control homeostasis and function of innate lymphoid cells
title_short Subset- and tissue-defined STAT5 thresholds control homeostasis and function of innate lymphoid cells
title_sort subset- and tissue-defined stat5 thresholds control homeostasis and function of innate lymphoid cells
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5626390/
https://www.ncbi.nlm.nih.gov/pubmed/28916644
http://dx.doi.org/10.1084/jem.20150907
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